Transgenic mouse over-expressing calreticulin (CRT) in vascular smooth muscle cells

ABSTRACT

A transgenic mouse whose genome comprises a transcriptional control region operably linked to a cDNA encoding calreticulin (CRT) is described.

PRIOR APPLICATION INFORMATION

[0001] This application claims priority on U.S.SNo. 60/455,399, filed Mar. 18, 2003.

FIELD OF THE INVENTION

[0002] The present invention relates generally to the field of animal models for human diseases. More specifically, it relates to a transgenic mouse usable as an animal model for hemangioendothelioma.

BACKGROUND OF THE INVENTION

[0003] Transgenic mice technology involves the introduction of new or altered genetic material into the mouse germ line. This results in lineages that carry the new integrated genetic material.

[0004] Endoplasmic reticulum (ER) plays an important role in many functions of the cell. ER is not only the protein folding and processing machinery of the cell but it plays an important role in Ca²⁺ storage and regulation of intracellular Ca²⁺ homeostasis (Pozzan et al., 1994). It is also important in gene regulation (unfolded protein response) (Tirasophon et al., 1998; Welihinda et al., 1997). There are a number of ER resident proteins (including CRT) which are essential for the proper implementation of these functions.

[0005] Studies on tumor angiogenesis have resulted in a significant progress in our understanding of the genetic and molecular mechanisms that control the development of the vascular system. The embryonic origin of the vascular system is best understood with respect to endothelial cells (Cleaver and Krieg, 1999). These cells are the defining cell types of the vascular system. During embryogenesis, these cells differentiate (from angioblast origin), migrate, and assemble into the vascular network. Subsequently pericytes are recruited to the periphery of the endothelium and differentiate into vascular smooth muscle cells (Manasek, 1971).

[0006] The formation of the vascular system is achieved by the coordination of two processes, namely vasculogenesis and angiogenesis (Risau and Lemmon, 1988), (Pardanaud et al., 1989). Vasculogenesis is the first step in vascular development leading to layout of the initial primitive vascular network, the capillary plexus (Risau and Flamme, 1995). Angiogenesis is a later process, which involves the sprouting, branching and differential growth of blood vessels to form the mature vessel (Risau and Flamme, 1995). There are two types of angiogenesis: sprouting angiogenesis, involving true sprouting of capillaries from preexisting blood vessels, and non-sprouting angiogenesis (or intussusception) which involves the splitting of preexisting vessels (Folkman and Klagsbrun, 1987; Klagsbrun and D'Amore, 1991; Patan et al., 1996). Vascularization of tissues like the yolk sac, embryonic brain, kidney, thymus, limb bud and intersomitic vessels are formed by sprouting angiogenesis (Ekblom et al., 1982; Le Lievre and Le Douarin, 1975; Bar, 1980; Joterau and Le Douarin, 1978; Stewart and Wiley, 1981; Coffin and Poole, 1988). However, in the developing lung, myocardium, chorioallantoic membrane, endothelial wound healing and the development of coronary arteries, vascularization occurs by non-sprouting, or intussusception angiogenesis (Flamme and Risau, 1992; Burri and Tarek, 1990; van Groningen et al., 1991; Patan et al., 1993; Patan et al., 1996; Reidy and Schwartz, 1981; Bogers et al., 1989).

[0007] A large number of molecules can affect angiogenesis and vasculogenesis, including a number of growth factors, their receptors, and components of the extracellular matrix (ECM) (reviewed in Cleaver and Krieg, 1999). The receptor tyrosine kinases expressed on the surface of endothelial cells also play important roles in initiating the program of endothelial cell growth during development and subsequent vascularization during wound healing and tumorigenesis. VEGF and its receptor Flk-1 are thought to be responsible for both primary vessel formations during vasculogenesis and angiogenic invasion of the developing organs (Flamme et al., 1995; Cleaver et al., 1997; Cleaver and Krieg, 1999). Both Flk-1 and Flt-1 (placental growth factor receptor) are expressed exclusively in the endothelial cells (Flamme et al., 1995; Peters et al., 1993). Tie-2 is another receptor tyrosine kinase which is highly expressed in the endothelial cells during embryogenesis and adult life (Davis et al., 1996; Suri et al., 1996). This receptor and its ligands, angiopoietin-1 and 2, are involved in angiogenesis and later vascular remodeling (Dumont et al., 1995; Sato et al., 1995). Targeted disruption of the Tie-2 gene in mice resulted in embryonic lethality due to defects in the integrity of the endothelium, and consequently defects in cardiac and vascular development (Dumont et al., 1992; Dumont et al., 1994; Dumont et al., 1995). These observations demonstrate that the Tie-2 signaling pathway plays a critical role in the differentiation, proliferation, and survival of endothelial cells as well as heart development in the mouse embryo (Dumont et al., 1994; Sato et al., 1995). Because gene targeted deletion of CRT results in similar cardiovascular defects in the embryos (Mesaeli et al., 1999), one may hypothesize that CRT plays a role in the growth factor signaling pathway. Indeed, an inverse relationship between expression of CRT and total cellular tyrosine phosphorylation level has been reported in cultured cells (Fadel et al., 1999) suggesting that the protein may affect tyrosine phosphorylation-dependent signaling.

[0008] The ECM and cell adhesion proteins can also regulate the process of vasculogenesis and angiogenesis by modulating growth, differentiation and migration of the endothelial cells (Risau and Lemmon, 1988; Ausprunk et al., 1991). For example, fibronectin is essential for the assembly of the vessel (Risau and Lemmon, 1988; Hynes, 1990), while collagen and laminin become important in later stages of vessel development (Hynes, 1990). Blocking of α₅β₁ integrin function results in major defects in early vasculogenesis (Drake et al., 1992; Yang et al., 1993). Blocking the β₃ family of integrins results in defects in angiogenesis and vascular cell survival (Brooks et al., 1994a; Brooks et al., 1994b). CRT may influence vessel formation through regulating the expression and function of cell adhesion proteins. For example differential expression of CRT affects integrin function (Leung-Hagesteijn et al., 1994; Coppolino et al., 1997). In addition, overexpression of CRT results in up-regulation of vinculin and N-cadherin (Fadel et al., 1999; Opas et al., 1996). It is still presently unclear if CRT alters angiogenesis through an effect on ECM or cell adhesion proteins or both.

SUMMARY OF THE INVENTION

[0009] According to a first aspect of the invention, there is provided a transgenic mouse whose genome comprises

[0010] a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin (CRT) wherein said control region comprises a promoter

[0011] wherein expression of calreticulin in the vascular smooth muscle cells (VSMC) results in hemangioma formation.

[0012] According to a second aspect of the invention, there is provided a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin wherein said control region comprises a SM22α promoter.

[0013] According to a third aspect of the invention, there is provided a method for producing a transgenic mouse whose genome comprises CRT comprising:

[0014] introducing into a fertilized mouse egg a transgene comprising a transcriptional control region operably linked to a cDNA encoding CRT wherein said control region comprises a promoter;

[0015] transplanting the injected egg in a foster parent female mouse; and

[0016] selecting a mouse derived from an injected egg whose genome comprises CRT.

[0017] According to a fourth aspect of the invention, there is provided a method for screening compounds that inhibit vascular tumor formation in a transgenic mouse comprising

[0018] providing a transgenic mouse whose genome comprises a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin (CRT);

[0019] allowing CRT to be expressed in VSMC of said transgenic mouse administering a compound to said mouse; and

[0020] determining whether said compound reduces hemangioma formation.

[0021] According to a fifth aspect of the invention, there is provided a method of testing the therapeutic activity of a pharmacological agent on hemangioenothelioma comprising administering an effective amount of said pharmacological agent to the mouse described above and evaluating said agent's effect on hemangioma formation of said mouse. In some embodiments, the hemangioenothelioma may be Kaposiform hemangioenothelioma.

[0022] According to a sixth aspect of the invention, there is provided a method of inhibiting hemangioma formation comprising administering an effective amount of a matrix metalloproteinase inhibitor to a patient in need of such treatment. Chemical inhibitors of matrix metalloproteinase include MMP-2/MMP-9 inhibitor I (2R)-2-[(4-Biphenylylsulfonyl)amino]-3-phenylpropionic Acid, IC₅₀=240-350 nM), MMP-2/MMP-9 inhibitor II (IC₅₀=17-30 nM), MMP-2/MMP-9 inhibitor III (IC₅₀=10 μM), and Chlorhexidine (Dihydrochloride). Alternatively, adeno-associated virus can be used to deliver the cDNA of TIMP-1 (Tissue inhibitor of matrix metalloproteinase) or TIMP-2 intravenously.

[0023] Patients diagnosed with hemangioendothelioma due to the presence of skin lesions (red/blue nodule on the skin at early cases) or deep soft tissue tumor can be treated with these inhibitors and the effect on the tumor size and progress could be studied over time.

[0024] According to a seventh aspect of the invention, there is provided a method of inhibiting hemangioma comprising administering to an individual in need of such treatment an effective amount of virally-administered small interference RNA (SiRNA) corresponding to a portion of CRT mRNA, wherein expression of the SiRNA decreases the level of CRT. The siRNA will be generated corresponding to the nucleotide 1916-1936 of the DNA sequence in FIG. 16 (sequences of sense 5′-GCU GAU CGU GCG GCC GGA CAA dTT 3′, and anti-sense 5′-UUG UCC GGC CGC ACG AUC AGC dTT 3′). This siRNA has been shown to significantly diminish the expression of CRT (Troussard et. al., 2003)

BRIEF DESCRIPTION OF THE DRAWINGS

[0025]FIG. 1—Schematic diagram showing the possible mechanism for the development of hemangioendothelioma in the SMCRT mice. Yellow boxes are items which will be tested.

[0026]FIG. 2. PCR and western blot showing the genotype and the expression of HA-CRT in the tissue from SMCRT transgenic (Tg) mice and non transgenic litter-mate (Non-Tg). A) Genomic DNA isolated from tail biopsy was used as a template for PCR with primers for HA and CRT cDNA. B) A piece of tail biopsy (containing tail vessels) or descending aorta was homogenized in RIPA buffer, containing protease inhibitors, and centrifuged to remove cellular debris. 20 μg of protein was then separated on 10% SDS acrylamide gel and transferred to nitrocellulose membrane. Membranes were probed with a polyclonal anti-HA antibody.

[0027]FIG. 3. Skin hemangioma in two lines of the SMCRT transgenic mice. The mouse in A showing the presence of smaller skin lesion, it also had a hemangioendothelioma in the chest originating from the aorta. B and C are images of the same mouse showing a larger hemangioma on the skin. This mouse was anesthetized and shaved to be able to see the size of the tumor. Arrows in C shows some of the skin vasculature surrounding the tumor. This mouse also had a large tumor originating from the heart which has also invaded the lungs.

[0028]FIG. 4. Histological structure of the Lungs from the wild type (A, B, C) and SMCRT (D, E, F) age matched mice. The SMCRT lung is congested and there is less alveolar spaces. Images are taken at three different magnifications (A, D) at 10×, (B, E) are at 20× and (C, F) are at 40×.

[0029]FIG. 5. Picture of the kidney (A) from a SMCRT mouse showing hemorrhage from the renal vessels and sub-capsule bleeding (blood clot, arrows) in the kidney. (B, C) show histology of the kidney from an adult wild type and SMCRT mice kidneys, zooming on the kidney cortex and capsule. Arrows in (C) shows the accumulation of blood in the kidney capsule of the SMCRT kidney. Arrowheads in B,C show the normal tissue of the kidney cortex.

[0030]FIG. 6. Histological structure of the kidney from wild type (A, B, C, D) and a SMCRT mouse (E, F, G, H). (A, B) and (E, F) are images from the medulla of the kidney, arrow heads pointing to the kidney tubules in the inner medulla while arrows in (E, F) points to the blood accumulation in the medulla and necrotic region. (C, D) and (G, H) are images from the kidney outer medulla. Arrows in (G, H) show the necrotic area and bleeding in this region of the SMCRT, while the arrow heads show the normal tissue.

[0031]FIG. 7. Histological structure of the kidney glomeruli from wild type (A) and a SMCRT mouse (B). Arrows in B point to accumulation of blood in the glomeruli of the kidney of the SMCRT mice. This could be due o formation of thrombus in the glomerulus of the kidney.

[0032]FIG. 8. Heart and coronary artery structure in (A) wild type and (B, C) transgenic mice overexpressing calreticulin in the vascular smooth muscle cells (SMCRT). (A) and (B) are hearts freshly isolated from age-matched mice, while the heart in (C) is a picture from a formalin preserved heart. In the SMCRT hearts there is an increased coronary artery vascularization (arrowheads in B). The SMCRT hearts were also dilated as compared to wild type hearts. As seen in (C) we also observed ruptured coronary artery in some of the hearts from end stage of disease (mouse were dying) (Arrow in C).

[0033]FIG. 9. Histological section from a papillary muscle in the heart of wild type (A, B) and SMCRT transgenic mice (C,D). A and C are at 20× magnification while B and D are at higher magnification (40×). The SMCRT heart muscle (C,D) shows increased interstitial spaces between the muscle fibers and around the coronary artery when compared to the wild type heart muscle (A,B).

[0034]FIG. 10. Giant hemangioma associated with the hearts isolated from two different lines of transgenic mice overexpressing calreticulin in the vascular smooth muscle cells (SMCRT) (B,C). A and B are images of the same heart showing the size of the hemangioma. This structure appears in all the SMCRT mouse lines we have (4 different lines). It increases in size by age. The heart in (C) was isolated from one SMCRT mouse before it showed the symptoms of heart failure, and the picture was taken from freshly isolated tissue. Arrows in (D) and (E) show the origin of this hemangioma to be from the aorta (in two different heart). Arrowhead in (E) points to the dilated coronary artery in this heart. F) shows a higher magnification of this structure. All tissues in (A, B, D and F) were preserved in formalin. L=Lung, Ha=Hemangioma, V=ventricle

[0035]FIG. 11. Histology of the giant heamangioma (hemangioendothelioms) shown in FIG. 10F. (A, B, C, D) show different cell types found in the lumen of this tumor. Arrow heads in (A), (B) and (D) show cells which look more like epithelial cells, while the arrow head in C show other cell type which resemble mesenchymal cells. The blue arrows in A,B, and C show the red blood cells which is also part of this tumor. The surface of this tumor is covered with a single layer of cells resembling endothelial cells (Arrows in E and F). This hemangioendothelioma also contains lumen like-structures (D) which are lined by endothelial-like cells (arrows in D).

[0036]FIG. 12. Histological structure of coronary artery (A, A′, B, B′) and a kidney arteriole (C, C′, D, D′). The upper panel (A, A′ and C, C′) are from a wild type mouse and the lower panel (B, B′, C, C′) are from a SMCRT mouse. As seen in (B, B′) there is a larger interstitial space between the coronary artery and the myofibers in the SMCRT mouse as compared to the wild type (A,A′). The same can also be seen in the kidney arteriole from the SMCRT mouse compared to the wild type. Higher magnification images of the arterial walls (A′, B′, C′, D′) show some changes in the structure of the vessel wall. To understand the nature of these changes we will use immunohistochemistry to analyze the expression of the extracellular matrix proteins.

[0037]FIG. 13—Masson Trichrome staining of lung sections of wild type (A) and SMCRT (B), showing the changes in the arteriole walls of the transgenic mice. Arrows (Green) indicates the disruption in the smooth muscle layer and migration of the endothelial cells thus developing a pouch containing red blood cells (lined by the arrow heads in B) which can lead to the formation of hemangioma.

[0038]FIG. 14—Western blot analysis showing connexion 43 expression in the vascular smooth muscle cells (A) and hearts (B) isolated from the wild type and SMCRT mice. There was a significant decrease in the connexion 43 protein in the transgenic mice as compare to the wild type mice.

[0039]FIG. 15. Gelatin Zymography detecting the MMP-2 and MMP-9 activity in liver (A) and lung (B) tissue isolated from the wt and SMCRT mice. C) shows the activity of MMP-2 in the culture media from the wt and SMCRT smooth muscle cells detected by gelatin zymography. Briefly, cells were cultured in DMEM containing Insulin and transferrin for 24 hrs. 30 μl of media from culture plate with no cells (Media), wt cells and SMCRT cells (or 30 μg protein from each tissue) were separated on 7.5% SDS-acrylamide gel containing 1 mg/ml Gelatin. After removal of SDS from the gel (to re-nature the proteins), it was incubated in zymography buffer overnight at 37° C. The gels were then stained with Coomassie Blue and de-stained. The white bands represent the activity of MMP in the sample.

[0040]FIG. 16—Nucleotide and amino acid sequence of SM22α-CRT (SEQ ID No. 1).

[0041]FIG. 17—Nucleotide and amino acid sequence of SM22α-CRT-HA (SEQ ID No. 2).

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0042] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned hereunder are incorporated herein by reference.

[0043] As used herein, “calreticulin” or CRT, depending on the context, refers to a peptide encoding CRT as shown in FIG. 16 or 17, a cDNA encoding CRT as shown in FIG. 16 or 17, a cDNA molecule deduced from said peptide sequence, or a bioactive fragment or mutant or variant, either inter-species or intra-species, form thereof. As will be appreciated by one of skill in the art, a variant may be CRT from a different species which has at least 60% homology, or at least 70% homology or at least 80% homology to CRT amino acid sequence shown in FIG. 16 (SEQ ID No.3) or is a peptide known or believed to be related to or functionally homologous to CRT or a bioactive fragment thereof. As used herein, “bioactive” with regard CRT indicates that the fragment or mutant form of CRT retains substantially normal or biological CRT activity.

[0044] As used herein, “Kasbach-Merritt Syndrome” refers to a syndrome characterized by very extensive and progressively enlarging vascular malformation that may involve large portions of the patient's extremities. In this syndrome, bleeding is secondary to disseminated intravascular coagulation triggered by stagnant blood flow through the tortuous vessels.

[0045] As used herein, “hemangiomas” refer to tumor-like clusters of proliferating capillaries or abnormally dense collections of dilated small blood vessels that occur in skin or internal organs. Hemangiomas may be for example surface hemangiomas or cavernous hemangiomas. Kaposiform hemangioendothelioma (KHE) refers to a very aggressive form of hemangioma, often accompanied by platelet trapping and thrombocytopenia.

[0046] As used herein, “hemangioendothelioma” refers to proliferative and neoplastic vascular lesions, including hemangiomas.

[0047] Described herein is the preparation of a transgenic mouse arranged to express calreticulin (CRT) in vascular smooth muscle cells. This results in a mouse having symptoms similar to Kasbach-Merritt Syndrome. By expressing CRT in vascular smooth muscle cells, transgenic mice usable as animal models for hemangioendothelioma can be prepared. That is, the transgenic mouse can be used to study many aspects of hemangioendothelioma, including the molecular mechanism of tumor formation, cell type involvement and efficacy of potential treatments.

[0048] The CRT is stably integrated within the SMCRT mouse genome, meaning that any offspring mice will express the same traits as their parents. Thus, the obtained transgenic mice can be used to conduct experiments with extremely high reproducibility.

[0049] In one embodiment of the invention, there is provided a transgenic mouse whose genome comprises a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin (CRT) wherein said control region comprises a promoter wherein expression of calreticulin in the vascular wall results in hemangioma formation. In some embodiments, the promoter is a vascular smooth muscle-specific promoter, for example, SM22α promoter. As will be appreciated by one of skill in the art, the cDNA encoding CRT may be as shown in FIG. 16 or may be deduced from the amino acid sequence of CRT as shown in FIG. 16. In other embodiments, the cDNA sequence within the transgene may include sequence variations, for example, mutations and deletions, which do not significantly affect or alter the normal, biological function of CRT.

[0050] In another embodiment of the invention, there is provided a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin wherein said control region comprises a SM22α promoter, as shown in FIG. 16. In another embodiment, the transgene includes a tag for distinguishing between transgenic CRT and endogenous CRT, as shown in FIG. 17 and as discussed below. In the embodiment shown in FIG. 17, the tag is HA although other suitable tags known in the art may also be used.

[0051] In another aspect of the invention, there is provided a method for producing a transgenic mouse whose genome comprises CRT comprising: introducing into a fertilized mouse egg a transgene comprising a transcriptional control region operably linked to a cDNA encoding CRT wherein said control region comprises a promoter; transplanting the injected egg in a foster parent female mouse; and selecting a mouse derived from an injected egg whose genome comprises CRT. As will be appreciated by one of skill in the art, the transgene may be introduced into the mouse egg by any of a number of suitable methods known in the art.

[0052] In another embodiment of the invention, there is provided a method for screening compounds that inhibit vascular tumor formation in a transgenic mouse comprising providing a transgenic mouse whose genome comprises a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin (CRT); allowing CRT to be expressed in said transgenic mouse administering a compound to said mouse; and determining whether said compound reduces hemangioma formation. In these embodiments, the hemangioma in the mouse treated with the compound may be compared to hemangioma in an untreated control and the difference between the treated mouse and untreated control used to determine efficacy of the compound. Examples of human vascular tumors include but are by no means limited to cavernous hemaginoma, Kaposi's sarcoma or those characterizing Kasabach-Merritt syndrome.

[0053] In one embodiment of the invention, there is provided a method of inhibiting hemangioma formation comprising administering an effective amount of a matrix metalloproteinase inhibitor to a patient in need of such treatment. As discussed below, transgenic mice expressing CRT show increased matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) activity compared to wild type mice. Thus, inhibiting MMP activity will accomplish at least one of the following: reduce frequency of hemangioma formation, reduce size and/or severity of hemangioma, inhibit or reduce hemangioma formation, and treat or ameliorate at least one symptom associated with hemangioma formation.

[0054] Chemical inhibitors of matrix metalloproteinase include but are by no means limited to MMP-2/MMP-9 inhibitor I (2R)-2-[(4-Biphenylylsulfonyl)amino]-3-phenylpropionic Acid, IC₅₀=240-350 nM), MMP-2/MMP-9 inhibitor 11 (IC₅₀=17-30 nM), MMP-2/MMP-9 inhibitor III (IC₅₀=10 μM), and Chlorhexidine (Dihydrochloride). Alternatively, adeno-associated virus can be used to deliver the cDNA of TIMP-1 (Tissue inhibitor of matrix metalloproteinase) or TIMP-2 intravenously. As will be appreciated by one of skill in the art, the concentrations provided above are for illustrative purposes only and the exact dosage that comprises an “effective amount” of an MMP inhibitor may vary according to the weight, health, age and/or overall condition of a patient, but will be the dosage that is sufficient to complete the intended purpose, that is, inhibit hemangioma formation as discussed above.

[0055] Patients diagnosed with hemangioendothelioma due to the presence of skin lesions (red/blue nodule on the skin at early cases) or deep soft tissue tumor can be treated with these inhibitors and the effect on the tumor size and progress could be studied over time.

[0056] In another embodiment of the invention, there is provided a method of inhibiting hemangioma comprising administering to an individual in need of such treatment an effective amount of virally-administered small interference RNA (siRNA) corresponding to a portion of CRT mRNA, wherein expression of the siRNA decreases the level of CRT. Efficient and stable expression of siRNA can be achieved by gene delivery using means known in the art, for example, using lentiviral plasmids which are available commercially (Invitrogen).

[0057] In another embodiment of the invention, there is provided a method of testing the therapeutic activity of a pharmacological agent on hemangioenothelioma comprising administering an effective amount of said pharmacological agent to the above-described transgenic mouse and evaluating said agent's effect on hemangioma formation of said mouse. As will be appreciated by one of skill in the art, the evaluation may comprise detecting for example a decrease in hemangioma size or formation compared to an untreated or mock-treated control. It is important to note that in the process, the control does not necessarily need to be repeated with each trial. It is of note that the pharmacological agent may be for example a peptide or peptide fragment, a small molecule, a chemical compound, a nucleic acid or the like.

[0058] Several lines of evidence suggest a role for calreticulin (CRT) in the process of angiogenesis by affecting cell adhesion, migration and proliferation. CRT is expressed in different cells of the vascular wall (Mesaeli and Michalak, 1995; Mesaeli et al., 1999; Milner et al., 1991; Tharin et al., 1992). CRT gene is also activated in the vascular bed early in mouse development (Mesaeli et al., 1999). Exogenously added CRT to the vascular cells or vessel lumen alters different aspects of vascular function. For example, in adult rats, exogenously added CRT acts as a vascular regulatory protein by reducing intimal hyperplasia (restenosis) after arterial injury (Dai et al., 1997). It also selectively inhibits endothelial cell proliferation when added to the endothelial culture media (Pike et al., 1999). Although these data postulate a role for CRT in the angiogenic process, direct evidence is not available. To investigate the role of CRT in vascular cell function, we generated a transgenic mouse overexpressing CRT in the vascular smooth muscle cells (hereafter will be referred to as SMCRT) using a truncated form of the SM22α promoter. These mice die at an adult stage. The overall symptoms of these mice are similar to the symptoms of the human patients with Kasabach-Merritt Syndrome. The main abnormality in the SMCRT mice is the development of “Giant hemangioma” associated with the outflow tract of the heart and the presence of hemangioma on the skin. Our results also show increased branching and vascularization of the coronary arteries accompanied by dilation of the heart. Other phenotypes of these mice are lung and kidney congestion (resembling congestive heart failure). In mice at an end stage of the disease, we have observed blood clots in the adipose tissue surrounding the kidneys and the presence of blood clots in the kidney capsule. These defects indicate vascular wall remodeling accompanied by increased microvascular permeability leading to tumor formation in these mice.

[0059] CRT is a ubiquitous eukaryotic protein which shares a high degree of identity among all the different species (Michalak, 1996). CRT is the product of translation of a single mRNA (Michalak, 1996), resulting in a 46 kDa protein which is localized to the lumen of ER and nuclear envelope (Michalak et al., 1992; Milner et al., 1992; Michalak, 1996). Several unique functions have been postulated for CRT (reviewed in Michalak et al., 1999), including chaperone activity (Nauseef et al., 1995; Nigam et al., 1994; Hebert et al., 1997), regulation of cell adhesion (Coppolino et al., 1995; Coppolino et al., 1997; Opas et al., 1996), modulation of steroid mediated gene expression (Burns et al., 1994; Dedhar et al., 1994; Michalak et al., 1996; Wheeler et al., 1995; Winrow et al., 1995), and regulation of Ca²⁺ homeostasis (Bastianutto et al., 1995; Camacho and Lechleiter, 1995; Coppolino et al., 1997; Liu et al., 1994; Mery et al., 1996).

[0060] Chaperone function of CRT—CRT is a lectin-like chaperone (Hammond and Helenius, 1995; Peterson et al., 1995; Spiro et al., 1996), involved in the “quality control” process during the synthesis and folding of a variety of proteins including cell surface receptors, integrins and transporters (Helenius et al., 1997). CRT binds the terminal glucose of the oligosaccharide moiety of the unfolded protein. During the folding process, the newly synthesized protein can go through many cycles of binding and release from the lectin-like chaperone by removal and addition of this terminal glucose (involving glucosidase I and II, and UDP-glucose transferase, respectively). This results in the proper processing of the protein. If the protein is misfolded, it will accumulate in the cell triggering an “unfolded protein response” and starting protein degradation. In the CRT null mouse embryonic fibroblast cells, we have observed an increase in the expression of a number of ER chaperones; however the function of these chaperones seems to be compromised (Mesaeli et al., 2000). Indeed, the unfolded protein response in these cells is stimulated as evident by a significant (100%) increase in the expression of BiP (Grp78) (Mesaeli et al., 2000). CRT has been shown to be bind to glycosylated laminin in the ER (McDonnell et al., 1996) perhaps affecting its folding. Overexpression of CRT has been shown to increase the level of pro-MMP2 protein (Ito et al., 2001). Other proteins which have been shown to be malformed in absence of CRT includes: bradykinin receptor (Nakamura et al., 2001b), MHC class I protein (Gao et al., 2002), IP₃ receptor (all three isoforms) (Paziuk and Mesaeli, 2002), and connexin 43 protein which fails to localize to the cell-cell junction in the heart (Ahmadi et al., 2002). Interestingly, overexpression of CRT in the hearts of transgenic mice resulted in a decrease in the expression of connexin 40 and 43 (Nakamura et al., 2001a).

[0061] CRT and cell adhesion—The first evidence for the possible role of CRT in cell adhesion came from in vitro studies designed to identify the cellular proteins which bind to KxFF(k/R)R peptide (Rojiani et al., 1991), a consensus sequence in the C-terminal tail of the α-subunit of integrin. However, recent reports indicate that CRT may influence cell adhesion indirectly via modulation of gene expression of adhesion related molecules (Fadel et al., 1999; Opas et al., 1996), or by changes in the integrin-dependent Ca²⁺ signaling (Coppolino et al., 1997). Overexpression of CRT results in up-regulation of vinculin and N-cadherin (Fadel et al., 1999; Opas et al., 1996), resulting in an increase in cell-substratum attachment. Down regulation of CRT results in an opposite effect (Leung-Hagesteijn et al., 1994; Opas et al., 1996). Protein tyrosine phosphorylation/dephosphorylation comprises one of the major mechanisms in regulating cell adhesion (Burridge and Chrzanowska-Wodnicka, 1996), (Cox and Huttenlocher, 1998; Daniel and Reynolds, 1997). Previously, we have reported a significant decrease in the level of tyrosine phosphorylation in fibroblast cells overexpressing CRT (Fadel et al., 1999) which coincided with changes in cell adhesiveness.

[0062] CRT and intracellular Ca²⁺—CRT was initially discovered as a Ca²⁺ binding protein in the lumen of ER (Ostwald et al., 1974), (Michalak et al., 1980). The protein has two Ca²⁺ binding sites: a high affinity, low capacity site and a low capacity, high affinity site (Ostwald et al., 1974), (Baksh and Michalak, 1991). Overexpression of CRT results in an increased level of intracellular Ca²⁺, however, it does not affect the cytosolic free Ca²⁺ concentration (Bastianutto et al., 1995), (Mery et al., 1996), (Michalak et al., 1996; Opas et al., 1996). Knockout of the CRT gene did not result in a change in the Ca²⁺ storage capacity of the ER in ES cells and in mouse embryonic fibroblast cells (Coppolino et al., 1997; Mesaeli et al., 1999). However, CRT deficient mouse embryonic fibroblast cells have decreased agonist-mediated IP₃-dependent Ca²⁺ release from ER (Mesaeli et al., 1999). CRT deficient ES cells also showed a defect in integrin mediated Ca²⁺ signaling (Coppolino et al., 1997). These results suggest a change in the expression of CRT can alter cellular Ca²⁺ homeostasis which in turn can affect many cell signaling pathways including cell adhesion (via integrin).

[0063] SMCRT transgenic mice—A truncated SM22α promoter (445 base pairs of the 5′ flanking region) which has been shown to target the Lac Z reporter gene expression in the vascular smooth muscle cells (specifically in the arterial side) but not other smooth muscle cells in the mouse embryo (Li et al., 1996) was used. We obtained this promoter from Dr. E. Olson (Southwestern Medical Centre, University of Texas, Dallas, USA) and cloned it upstream of mouse CRT cDNA tagged with HA epitope (HA-CRT). The epitope tag was used to differentiate between the expression of the transgene and the endogenous CRT. However, as will be appreciated by one of skill in the art, any suitable tag known in the art may be used if so desired. This plasmid was then used to generate a transgenic mouse overexpressing HA-CRT (SMCRT) in the vascular smooth muscle cells. The genotype of these mice was confirmed by PCR of the genomic DNA with primers specific to the sequence of SM22α (5′ primer) and CRT (3′ primer). The expression of the HA-CRT in these mice was detected using western blot with a polyclonal antibody to HA (FIG. 2). The heterozygous SMCRT mice develop abnormalities at an adult stage (about 4-10 months old). The older mice become lethargic and inactive. Most of the male heterozygous animals develop skin lesions (FIG. 3) and hemangioma which can be detected on the skin. These mice suffer from lung congestion (FIG. 4) and kidney thrombosis (FIG. 5), symptoms resembling congestive heart failure. The evidence of heart failure is also observed in older (10-12 months) female heterozygous mice. Analysis of the kidney of the SMCRT mice showed hemorrhage from renal vessels in the renal adipose tissue and the presence of thrombus inside the kidney capsules (FIG. 5A, C). Histological analysis of the kidneys from the mice at end stage disease showed necrosis in the kidney medulla and cortex (FIG. 6B, C). There was also increased blood accumulation in the kidney glomeruli (FIG. 7B) of the SMCRT mice as compared to the wild type glomeruli (FIG. 7A). This could result in thrombosis in glomeruli. Histological analysis (Hematoxylin/Eosin) of the lungs of these mice we have seen congestion of the lungs and accumulation of blood in the alveoli (FIG. 4).

[0064] There are also defects in the heart of the SMCRT mice including: heart dilation, increased vascularization of the coronary arteries and rupture of coronary artery in some of these mice (FIG. 8). We also observed changes in the ultrastructure of the myocardium (FIG. 9) with increased interstitial spaces. However, the major defect in these mice is the presence of Giant hemangioma in the chest (FIG. 10). The giant hemangioma originates from the base of the aorta (FIGS. 10D and E). We have 4 different lines of the SMCRT transgenic mice and all four develop the giant hemangioma. The overall symptoms of these mice are similar to the Kasabach-Merritt Syndrome, the pathology of which includes: giant hemangioma with consumptive coagulopathy disseminated intravascular coagulation, and congestive heart failure. The Kasabach-Merritt Syndrome is more common in female infants. However, in the SMCRT mice the earliest evidence for the development of hemangioma we observed was at 3 months old male mice. Recently, Kasabach-Merritt Syndrome has been associated with two distinct vascular tumors: the Kaposiform hemangioendothelioma and tufted angiomas (Enjolras et al., 1997). Tufted angioma is a benign slow growing angioma found in young patients which is localized to the skin and subcutaneous tissue (Jones and Orkin, 1989). The Kaposiform hemangioendothelioma is an aggressive vascular tumor which can occur in soft tissue of the trunk, extremities and retroperitoneum (for review see Gampper and Morgan, 2002). The hemangioendothelioma occurs with similar frequency in both sexes and can develop at birth or later in life (Gampper and Morgan, 2002). This vascular tumor is associated with a high mortality rate and treatment is often inadequate (Powell, 1999). The histopathology reports on the Kaposiform hemangioendothelioma show that this tumor is surrounded by a thin-walled vessel lined by endothelial cells and filled with erythrocytes, thrombus, and sheets of cells (epithelioid and mesenchymal) (Perkins and Weiss, 1996). The molecular mechanism of development of the hemangioendothelioma is not known.

[0065] Histological analysis (Hematoxylin/Eosin) of the hemangioendothelioma isolated from the heterozygous SMCRT mice (FIG. 11) shows the presence of a vessel like structure covered with a layer of cells resembling endothelial cells (FIG. 11E, F). We also observed the appearance of several lumen-like structures inside this tumor which is also lined with endothelial-like cells (FIG. 11D). The presence of blood cells (blue arrows in FIGS. 11A, B and C) and different types of cells (resembling epithelial cells, Arrow head in FIG. 11A, 11B, 11D and mesenchymal cells Arrow head in FIG. 11C) were also detected. Histological sections of coronary artery (FIG. 12A) and kidney arteriol (FIG. 12B) shows an increase in the connective tissue around these vessels and changes in the structure of the smooth muscle layer of these vessels. The increased expression of CRT in the vascular smooth muscle cells results in the disruption of the smooth muscle layer (FIG. 13B, C). These changes lead to activation of the endothelial cells to proliferate and migrate through the smooth muscle cells (FIG. 13 C) resulting in the formation of hemangioendothelioma. The observed defects in the SMCRT mice indicate vascular wall remodelling which could cause the increased permeability of blood vessels in the SMCRT mice. Also the presence of such a large tumor in the vascular system can cause changes in the intravascular pressure (leading to hypertension) which can also result in some of the observed defects. Indeed one case report showed the development of hemangioendothelioma from thoracic aorta of a 54 years old woman which led to aortic obstruction, hypertension and congestive heart failure (Traverse et al., 1999). Therefore, we will study changes in blood pressure in these mice. The SMCRT mouse is a unique mouse model which is proving very interesting and to our knowledge is the only animal model for the hemangioendothelioma.

[0066] To identify all the cell types involved in the formation of this tumor we will use cell specific antibodies for immunohistochemical staining. We will isolate the tumor and areas of the skin with hemangioma from the SMCRT mice. This tissue will be fixed in 4% paraformaldehyde and processed for freezing in Tissue Tec as described previously (Mesaeli et al., 1999). Thin cryosections (7-10 μm) will then be prepared and incubated with the following antibodies: CD31, CD34 (BD Biosciences) and von Willebrand factor (Dako) as endothelial markers, smooth muscle actin (Sigma), vimentin as mesenchymal cell marker (Chemicon) and RTU-ESA (Vector Laboratories) as epithelial specific marker. This staining will be followed by FITC (or Texas red) labeled secondary antibodies. The nuclear stain DAPI will be used to localize the nuclei in each section. The confocal images from the FITC (or Texas red) signal and DAPI will then be superimposed to study the localization of the cells. We are using three different markers for endothelial cells because previous report has showed variability in the expression of these endothelial markers in the hemangioendothelioma (Mentzel et al., 1997).

[0067] Our observation of the accumulation of blood in the kidney glomeruli and lungs implies an increase in the permeability of the vasculature in the SMCRT mice. Therefore, to test for the changes in the microvascular permeability in different tissues we will use fluorescently labeled albumin following the protocols described previously (Harris et al., 2002). We will label albumin (Sigma) with FITC using the FluoroTag FITC Conjugation kit (Sigma). In brief, albumin (10 mg/ml) and FITC powder will be dissolved in carbonate-bicarbonate buffer. The FITC solution will be added slowly to the BSA and mixed for 2 hrs. The FITC-BSA conjugate will be separated from the free FITC by a G25 column. I have used this system previously for FITC labeling of CRT (Dai et al., 1997). The FITC-albumin or FITC alone will be injected in the tail vein of the transgenic SMCRT and non-transgenic litter mate mice. After 30 min (Harris et al., 2002), these mice will be euthanized, lung, kidney, skin and heart will be collected and fixed for 10 min in 4% paraformaldehyde followed by freezing. Thin cryostate sections (6-10 μm) will be generated. These sections will be mounted in a mounting media containing DAPI (a nuclear marker) to localize the cell nuclei. The fluorescence in these sections will then be analyzed. If there is an increase in vascular permeability we should see the FITC-albumin conjugate in the extravascular spaces.

[0068] One of the pathological diagnoses associated with hemangioendothelioma is disseminated intravascular clotting associated with thrombocytopenia (decreased platelet count in circulating blood). Decreased levels of platelets, procoagulant proteins and protease inhibitors is the result of activation of the coagulation, degradation of coagulation factors accompanied by decreased synthesis of these factors. As shown in FIG. 5, 8, 9 we have observed an increase in the thrombus formation in different tissue of the SMCRT mice. Thus it is important to examine the changes in the blood clotting and factors involved in this process in these mice. We will examine CBC (blood cell count, and morphology), platelet counts, clotting time and hematocrit values. Furthermore, we will test the platelet aggregation characteristics in platelet rich fraction of blood from the SMCRT and wild type mice. If we find changes in the platelet aggregation we will then evaluate the expression level of different proteins involved in the blood clotting pathway. We will use western blot analysis to test the level of fibrinogen, thrombin, Factor VIII and X. These tests will help us to identify the mechanism resulting in formation of thrombus in different tissues.

[0069] To date all of the samples we analyzed were isolated from adult mice with fully developed disease or at end stage. Because in human this disease can also be found at an early age (found from 6 months to 74 years of age) (Gampper and Morgan, 2002; Powell, 1999), we will determine when this tumor starts developing in the SMCRT mice. Thus we will carry out an age dependent study. In these studies we will use mice at different age starting from late embryonic age (E17 and E19), neonate (2 days), 1, 5 and 8 months old SMCRT mice. These mice will be first checked for the appearance of skin changes. They will then be euthanized and tumor, heart, major arteries (aorta, thoracic artery, and renal artery), lung and kidneys will be used for histological analysis.

[0070] A summary of the possible mechanisms for the development of hemangioendothelioma in the SMCRT mice is outlined in FIG. 1. In the arterial wall of these mice the vascular smooth muscle cells (VSMC) are overexpressing CRT, while the endothelial (and other cells) have their basal expression of CRT. In the vessel wall, there is a dynamic interaction between the VSMC and the endothelial cells through the basement membrane which is made predominantly from collagen IV, laminin and heparan sulfate proteoglycans. A second layer of ECM known as interstitial matrix and is made from fibrillar collagen and fibronectin surrounding the VSMC and pericytes. Any change in the composition of these ECM will disturb the vessel wall structure. In the SMCRT vessel wall, the changes in the VSMC can be on multiple levels. We postulate a change in the composition of the ECM surrounding the VSMC cells due to either their decreased expression or increased degradation by active proteases. Indeed, overexpression of CRT has been shown to increase the secretion and activation of pro-MMP2 protein (Ito et al., 2001). CRT has also been shown to bind glycosylated laminin in the ER (McDonnell et al., 1996) perhaps affecting its folding. Previously we have showed that overexpression of CRT results in increased cell spreading and adhesion (Opas et al., 1996; Fadel et al., 1999). Thus we anticipate an increased expression of adhesion proteins in the VSMC causing them to attach to the ECM and spread. Loss of cell-cell contact proteins in VSMC can result in an increased permeability of the vessel wall. Gap junctions are one of the means of cell-cell contacts between the VSMC and endothelial cell (Little et al., 1995; Xia et al., 1995). Connexin 37, 40 and 43 are the main gap junction proteins present in both VSMC (Arensbak et al., 2001; Cai et al., 2001; van Kempen and Jongsma, 1999) and endothelial cells (Delorme et al., 1997; Simon and McWhorter, 2002; van Kempen and Jongsma, 1999). A recent report by Nakamura et al., (Nakamura et al., 2001a) showed that overexpression of CRT in the heart results in a significant decrease in the expression of connexin 40 and 43 in the cardiomyocytes. Indeed, we observed a significant decrease in the connexion 43 expression in vascular smooth muscle cells derived from the descending aorta (FIG. 14A) and in the hearts (FIG. 14B) of the SMCRT mice as compared to the wild type. Decreased connexin expression in the VSMC can result in altered communication via gap junction between the VSMC and endothelial cells thus affecting their function.

[0071] The endothelial cells of the SMCRT vessel wall express basal level of CRT and according to the above predicted changes they are faced with a change in the ECM. Changes in the ECM have been shown to induce endothelial cell to release growth factors (Dvorak et al., 1995), thus increasing the rate of endothelial cell proliferation (Underwood et al., 1998) and migration (Seeger et al., 2002). Collectively the changes in the ECM and the endothelial layer of the vessel wall activate platelet adhesion to the vessel wall (Balleisen and Rauterberg, 1980) leading to platelet aggregation and blood clotting. Evidence of thrombus formation in different tissues of the SMCRT mouse (tumor, kidney and lung) has been observed. Adhesion of platelets to the vessel wall and formation of fibrin (by breakdown of fibrinogen) in the blood clot will also result in release of growth factors (Campbell et al., 1999; Tezono et al., 2001) in this site leading to increased endothelial cell proliferation and migration. This further activates the angiogenic process and formation of the tumor in these mice.

[0072] We are studying the mechanism of development of this tumor (hemangioendothelioma) with emphasis on role of CRT in the development of this disorder. It is known that hemangioendothelioma develops as a result of biphasic proliferation and migration of endothelial cells to form dilated vessels which is filled with erythrocytes, thrombus with latter invasion of epithelioid and mesenchymal cells (Perkins and Weiss, 1996). One of the mechanisms that overexpression of CRT in smooth muscle cells can lead to the vascular wall changes which cause the development of this tumor could be via altering the expression of the extracellular matrix (ECM) and adhesion molecules rendering the vessel walls leaky. The change in the local composition of ECM in-vessel wall in addition to the shear force in the vessel wall has been shown to govern the ability of the endothelial cells to proliferate, migrate, differentiate and/or undergo apoptosis (Reviewed in Ingber, 2002). In the SMCRT mice the development of hemangioendothelioma depends on the abnormal cell growth and migration. Using histological techniques (Masson Trichrome, FIG. 13B,C) we observed that the increased expression of CRT in the vascular smooth muscle cells leads to changes in this layer of the vessel wall leading to activation of endothelial cell proliferation and migration (FIG. 13C arrow). These changes in the endothelial cells could be the cause of development of hemangioma and increased angiogenesis observed in the SMCRT mice.

[0073] Collagen (types I, III and IV) and elastin (mainly present in resistant arteries) are the major protein component of the ECM in the vessel wall (van der Rest and Garrone, 1991; Rosenbloom et al., 1993). Thus, in the initial experiments we will stain the paraffin embedded sections of different tissues of SMCRT and wild type mice with Van Gieson's Picric Acid stain to determine the changes in the collagen deposit in the microvasculature of different tissues. To detect the elastic fibers we will use the Elastic Stain (Sigma) which is a hematoxylin based stain. Staining of the paraffin sections will enable us to obtain good histological (and ultrastructural) details. Second, we will determine the temporal and spatial expression of ECM proteins including: elastin, collagen (I, III and IV), fibronectin, and laminin in the vessel walls of the SMCRT mice. Western blot with antibodies (available from Chemicon and Calbiochem) to these specific proteins will be carried out on tissue homogenates from arteries, veins, myocardium, lung, kidney and the tumor. We will also carry out immunohistochemical staining of the SMCRT and wild type tissue sections with antibodies to ECM proteins. Tissues (listed above) will be fixed in 4% paraformaldehyde, embedded and frozen (as described in Mesaeli et al., 1999), then 10-15 μm cryostat sections will be cut. The sections will be stained with antibodies to collagen I, III, IV, laminin, fibronectin, (available from Sigma and Chemicon) followed by staining using Vectastain Elite ABC kit and Vector DAB substrate (Vector Labs Inc.). The nuclei will be counter stained with methylgreen or hematoxylin for ultrastructural determination.

[0074] The changes in the ECM are not only limited to changes in their expression, but also to the rate of turnover of these proteins. The turnover of ECM is essential for many processes including embryonic development, wound healing, tissue remodeling, and disease development (such as cancer and vascular disease). The turnover of ECM is mediated by the activity of different proteases including secreted matrix metalloproteinase (MMP). Because of the important function of MMPs in regulating cell migration and invasion, all the MMP are secreted as an inactive pro-MMP. A large number of MMP has been identified in different tissues, however only MMP-1, 2, 3, 7 and 9 have been reported in vascular tissue (Jacob et al., 2001). MMP-1 is a collagenase which is secreted by endothelial cells (Lin et al., 1997). MMP-2 and MMP-9, which are gelatinases, are secreted by endothelial and vascular smooth muscle cells (Gurjar et al., 1999; Ishii and Asuwa, 2000; Peracchia et al., 1997). MMP-7 is an elastase and has a low level of expression in the vascular wall (Jacob et al., 2001). The activities of these MMPs are tightly regulated by tissue inhibitor metalloproteases (TIMP). Four isoforms of TIMP have been found, TIMP-1 binds pro-MMP-9, TIMP-2 and -4 bind pro-MMP-2 (Brew et al., 2000). Therefore, we will examine for changes in the activity and the expression of MMPs and TIMPs in the arterial walls of the SMCRT mice and compare that to their wild type litter mate. In our preliminary data on MMP activity we used zymography techniques. As shown in FIG. 15A, the activity of both MMP-2 and MMP-9 are increased in the tissues isolated from the SMCRT mice as compared to wild type. In addition, we observed an increase in the MMP-2 activity in the primary smooth muscle cells isolated from the descending aorta from the transgenic mice as compared to the wild type mice (FIG. 15 B). To determine if these changes in the MMP activity is due to changes in the protein expression or a decrease in the TIMP level we will quantifying the expression of MMP-2, -9 and TIMP-1, -2, -4 using western blot analysis and specific antibodies to these proteins (Calbiochem). If there were changes in the protein levels, we will determine if these changes are due to an increase in the mRNA level using quantitative RT-PCR. We will also determine the cellular localization of these proteases using immunohistochemical techniques (as described above). Interestingly, Ito et al. has recently showed that overexpression of CRT in human rhabdomyosarcoma cells resulted in an increase in the secretion and activation of pro-MMP2 (Ito et al., 2001). However, no data is available on other MMP or TIMP expression or the activity of any of these proteases when the expression of CRT is altered. Therefore, we propose to study the activity of MMP-2 and MMP-9 in the serum and in the media from the primary vascular smooth muscle cell cultures isolated from the SMCRT and wild type mice. One disadvantage of using cultured VSMC is that these cells in culture undergo phenotypic changes. However, we are interested to measure the release of the MMP proteins from the VSMC layer only not the whole artery. Therefore, to avoid this setback we will only use the first passage of these cells (as we have done in FIG. 15B). In our experiments we have isolated vascular smooth muscle cells (VSMC) from the descending aorta of the SMCRT and wild type mice using explant techniques. Because the MMPs are secreted from the cells we will separate the media from these VSMC to test for their activity. We will also harvest serum from the SMCRT and wild type mice to test for MMP activity. The MMP assay (available from Chemicon) utilizes a biotinylated gelatinase substrate which is cleaved by the active MMP-2 or MMP-9. The remaining biotinylated fragments are then measured in a colorimetric ELISA based assay using a biotin-strepavidin complex.

[0075] Cell migration is essential during vascular development and vascular injury (Noden, 1988; Poole and Coffin, 1989). Once endothelial cells differentiate, they proliferate and migrate and assemble to generate the vascular network. Cell migration is also important in recruiting the smooth muscle cells to the endothelial tubes for maturation of the blood vessel. Endothelial cell migration is also important in branching of the vessels during the process of wound healing (Reidy and Schwartz, 1981) and in tumor angiogenesis (Sheu et al., 1997). In the development of hemangioendothelioma, endothelial cells and other cells (erythrocytes, epithelial and mesenchyme cells) have to migrate to form the tumor (Gampper and Morgan, 2002). How is this migration initiated? As outlined in FIG. 1, we propose that in the vessel wall of the SMCRT mice, the ECM structure is altered (perhaps by a decrease in the synthesis or accelerated degradation of ECM fibers). In these vessels, the endothelial cells (express only the endogenous level of CRT) will have less substrate (ECM) to adhere to thus promoting their migration, while VSMC will be more adherent and will not follow the migratory path of the endothelial cells. Indeed, previously we showed that overexpression of CRT renders the cells more adherent while decrease in CRT expression in these cells (using antisense oligo) resulted in less adhesion (Fadel et al., 1999). We also showed that overexpression of CRT in cultured cells increases the expression of vinculin and N-cadherin (adhesion proteins) (Opas et al., 1996). The SMCRT mouse model would be ideal to test the expression of different adhesion molecules in two different cell types expressing different levels of CRT. Here, we propose to measure the expression (by western blot) and localization (by immunohistochemistry) of different adhesion molecules including: integrins (α₂β₁, α_(v)β₃ and α₃β₁), vinculin, and cadherins in the vascular wall of the. SMCRT mice as compared to the wild type mice. To study cell migration, we will isolate smooth muscle cells from the SMCRT and wild type mice as described above. The rate of cell migration will be tested using Boyden chambers containing filters with a pore diameter of 8 μm (Costar, as described in Dai et al., 1997). Cell suspensions will be plated in the upper part of the chamber and incubated at 37° C. for 2-8 hours. The cells that migrate into the filters will be fixed, stained with Giemsa dye and counted. To test the effects of different ECM proteins (collagen, fibronectin, laminin) on the rate of cell migration, the wells will be coated with different substrates and the above experiments will be repeated.

[0076] To study the changes in the rate of cell proliferation in arterial wall and tumor in situ we will use bromo-2′-deoxyuridine (BrdU) to label newly synthesized DNA. Wild type and SMCRT mice will be injected intraperitoneally with 0.2 ml of 15 mg/ml BrdU (Roche Diagnostics) dissolved in 0.86% saline (Wigle et al., 1999). 2 hrs after injection these mice will be euthanized. We will harvest the tumor and the major thoracic arteries from the SMCRT mice, as a control we will isolate the major thoracic arteries from the wild type mice. These tissues will be fixed in 4% paraformaldehyde (PFA), frozen and cryosectioned. The sections will be denatured with 2N HCl and re-natured in 0.1M Sodium Borate buffer pH 8.5 to denature DNA (Wigle et al., 1999). Sections will then be stained with monoclonal antibody to BrdU (BD Biosciences) and visualized with a FITC-secondary antibody. To determine if there is a cell specific difference in the cell proliferation we will use cell specific antibodies as markers to double label the tissue sections. We will use anti-CD31, CD34 (BD Biosciences) and von Willebrand factor (Dako) as endothelial cell markers, and anti-smooth muscle actin (Sigma) for smooth muscle cells. Each antibody will be visualized by using a Texas-Red conjugated secondary antibody.

[0077] While the preferred embodiments of the invention have been described above, it will be recognized and understood that various modifications may be made therein, and the appended claims are intended to cover all such modifications which may fall within the spirit and scope of the invention.

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1 24 1 2655 DNA Artificial artificial construct of sm22a promoter and CRT cDNA 1 ccccttcctt cagatgccac aaggaggtgc tggagttcta tgcaccaata gcttaaacca 60 gccaggctgg ctgtagtgga ttgagcgtct gaggctgcac ctctctggcc tgcagccagt 120 tcctgggtga gactgaccct gcctgagggt tctctccttc cctctctcta ctcctttcct 180 ccctctccct ctccctctct ctgtttcctg aggtttccag gattggggat gggactcaga 240 gacaccacta aagccttacc ttttaagaag ttgcattcag tgagtgtgtg agacatagca 300 cagatagggg cagaggagag ctggttctgt ctccactgtg tttggtcttg ggtactgaac 360 tcagaccatc aggtgtgata gcagttgtct ttaaccctaa ccctgagcct gtctcacctg 420 tcccttccca agaccactga agctaggtgc aagataagtg gggacccttt ctgaggtggt 480 aggatctttc acgataagga ctattttgaa gggagggagg gtgacactgt cctagtcctc 540 ttaccctagt gtcctccagc cttgccaggc cttaaacatc cgcccattgt caccgctcta 600 gaaggggcca gggttgactt gctgctaaac aaggcactcc ctagagaagc acccgctaga 660 agcataccat acctgtgggc aggatgaccc atgttctgcc acgcacttgg tagccttgga 720 aaggccactt tgaacctcaa ttttctcaac tgttaaatgg ggtggtaact gctatctcat 780 aataaagggg aacgtgaaag gaaggcgttt gcatagtgcc tggttgtgca gccaggctgc 840 agtcaagact agttcccacc aactcgattt taaagccttg caagaaggtg gcttgtttgt 900 cccttgcagg ttcctttgtc gggccaaact ctagaatgcc tccccctttc tttctcattg 960 aagagcagac ccaagtccgg gtaacaagga agggtttcag ggtcctgccc ataaaaggtt 1020 tttcccggcc gccctcagca ccgccccgcc ccgacccccg cagcatctcc aaagcatgca 1080 gagaatgtct ccggctgccc ccgacagact gctccaactt ggtgtctttc cccaaatatg 1140 gagcctgtgt ggagtgagtg gggcggcccg gggtggtgag ccaagcagac ttccatgggc 1200 agggaggggc gccagcggac ggcagagggg tgacatcact gcctaggcgg cctttaaacc 1260 cctcacccag ccggcgcccc accgagctcg gatccactag tccagtgtgg tggaattc 1318 atg ctg ctc cct gtg ccg ctg ctg ctc ggc ctg ctc ggc ctg gcc gcc 1366 Met Leu Leu Pro Val Pro Leu Leu Leu Gly Leu Leu Gly Leu Ala Ala 1 5 10 15 gcc gag ccc gtc gtc tac ttc aag gag cag ttt ctg gac gga gat ggg 1414 Ala Glu Pro Val Val Tyr Phe Lys Glu Gln Phe Leu Asp Gly Asp Gly 20 25 30 tgg acc gag cgc tgg atc gaa tcc aaa cac aag tcc gat ttt ggc aaa 1462 Trp Thr Glu Arg Trp Ile Glu Ser Lys His Lys Ser Asp Phe Gly Lys 35 40 45 ttc gtc ctc agt tcg ggc aag ttc tac ggc gat cag gag aaa gat aaa 1510 Phe Val Leu Ser Ser Gly Lys Phe Tyr Gly Asp Gln Glu Lys Asp Lys 50 55 60 ggg ctg cag acc agc cag gac gcc cgc ttc tac gcc ctg tcg gcc cga 1558 Gly Leu Gln Thr Ser Gln Asp Ala Arg Phe Tyr Ala Leu Ser Ala Arg 65 70 75 80 ttc gag ccg ttc agc aac aag ggc cag cca ctg gtg gtg cag cca gcc 1606 Phe Glu Pro Phe Ser Asn Lys Gly Gln Pro Leu Val Val Gln Pro Ala 85 90 95 agg acg ccc gct tct acg ccc tgt cgg ccc gat tcg agc cgt tca gca 1654 Arg Thr Pro Ala Ser Thr Pro Cys Arg Pro Asp Ser Ser Arg Ser Ala 100 105 110 aca agg gcc agc cac tgg tgg tgc agt tca ccg tga aac acg agc aga 1702 Thr Arg Ala Ser His Trp Trp Cys Ser Ser Pro Asn Thr Ser Arg 115 120 125 aca ttg act gcg ggg gcg gct acg tga agc tgt ttc cgg ccg gcc tgg 1750 Thr Leu Thr Ala Gly Ala Ala Thr Ser Cys Phe Arg Pro Ala Trp 130 135 140 acc aga agg aca tgc acg ggg act ctg agt aca aca tca tgt ttg gtc 1798 Thr Arg Arg Thr Cys Thr Gly Thr Leu Ser Thr Thr Ser Cys Leu Val 145 150 155 ctg aca tct gtg gcc ccg gca cca aga agg ttc acg tca tct tca act 1846 Leu Thr Ser Val Ala Pro Ala Pro Arg Arg Phe Thr Ser Ser Ser Thr 160 165 170 aca agg gca aga acg tgc tga tca aca agg aca tcc gtt gca agg acg 1894 Thr Arg Ala Arg Thr Cys Ser Thr Arg Thr Ser Val Ala Arg Thr 175 180 185 acg agt tca cac acc tgt aca cgc tga tcg tgc ggc cgg aca aca cgt 1942 Thr Ser Ser His Thr Cys Thr Arg Ser Cys Gly Arg Thr Thr Arg 190 195 200 atg agg tga aga ttg aca aca gcc agg tgg agt cgg gct ccc tgg agg 1990 Met Arg Arg Leu Thr Thr Ala Arg Trp Ser Arg Ala Pro Trp Arg 205 210 215 atg act ggg act tcc tac ccc cca aga aga taa agg acc cag atg cct 2038 Met Thr Gly Thr Ser Tyr Pro Pro Arg Arg Arg Thr Gln Met Pro 220 225 230 cga agc ctg aag act ggg acg agc ggg cca aga tcg acg acc cca cgg 2086 Arg Ser Leu Lys Thr Gly Thr Ser Gly Pro Arg Ser Thr Thr Pro Arg 235 240 245 250 act cca agc ccg agg act ggg aca agc ccg agc aca tcc ccg acc cgg 2134 Thr Pro Ser Pro Arg Thr Gly Thr Ser Pro Ser Thr Ser Pro Thr Arg 255 260 265 acg cga aga agc ccg aag act ggg acg aag aaa tgg acg gag agt ggg 2182 Thr Arg Arg Ser Pro Lys Thr Gly Thr Lys Lys Trp Thr Glu Ser Gly 270 275 280 agc cgc cgg tga ttc aga acc ccg agt aca agg gtg agt gga agc cgc 2230 Ser Arg Arg Phe Arg Thr Pro Ser Thr Arg Val Ser Gly Ser Arg 285 290 295 ggc aga tcg aca acc ccg att aca aag gca cct gga tcc acc ccg aaa 2278 Gly Arg Ser Thr Thr Pro Ile Thr Lys Ala Pro Gly Ser Thr Pro Lys 300 305 310 tcg aca acc ccg agt act cgc ccg acg cta aca tct atg cct acg aca 2326 Ser Thr Thr Pro Ser Thr Arg Pro Thr Leu Thr Ser Met Pro Thr Thr 315 320 325 gct ttg ccg tgc tgg gct tgg acc tct ggc agg tca agt cgg gca cca 2374 Ala Leu Pro Cys Trp Ala Trp Thr Ser Gly Arg Ser Ser Arg Ala Pro 330 335 340 345 tct tcg aca act tcc tca tca cca acg atg agg cgt acg cag agg agt 2422 Ser Ser Thr Thr Ser Ser Ser Pro Thr Met Arg Arg Thr Gln Arg Ser 350 355 360 ttg gca acg aga cgt ggg gcg tca cca aga cgg ccg aga agc aga tga 2470 Leu Ala Thr Arg Arg Gly Ala Ser Pro Arg Arg Pro Arg Ser Arg 365 370 375 aag aca agc agg acg agg agc agc gga tga agg agg agg agg agg aga 2518 Lys Thr Ser Arg Thr Arg Ser Ser Gly Arg Arg Arg Arg Arg Arg 380 385 390 aga agc gga agg agg agg agg agg ccg agg agg acg agg agg aca agg 2566 Arg Ser Gly Arg Arg Arg Arg Arg Pro Arg Arg Thr Arg Arg Thr Arg 395 400 405 acg aca agg agg acg agg atg agg acg agg agg aca agg acg agg agg 2614 Thr Thr Arg Arg Thr Arg Met Arg Thr Arg Arg Thr Arg Thr Arg Arg 410 415 420 agg agg agg cgg ccg ccg gcc agg cca agg acg agc tgt ag 2655 Arg Arg Arg Arg Pro Pro Ala Arg Pro Arg Thr Ser Cys 425 430 435 2 123 PRT Artificial Synthetic Construct 2 Met Leu Leu Pro Val Pro Leu Leu Leu Gly Leu Leu Gly Leu Ala Ala 1 5 10 15 Ala Glu Pro Val Val Tyr Phe Lys Glu Gln Phe Leu Asp Gly Asp Gly 20 25 30 Trp Thr Glu Arg Trp Ile Glu Ser Lys His Lys Ser Asp Phe Gly Lys 35 40 45 Phe Val Leu Ser Ser Gly Lys Phe Tyr Gly Asp Gln Glu Lys Asp Lys 50 55 60 Gly Leu Gln Thr Ser Gln Asp Ala Arg Phe Tyr Ala Leu Ser Ala Arg 65 70 75 80 Phe Glu Pro Phe Ser Asn Lys Gly Gln Pro Leu Val Val Gln Pro Ala 85 90 95 Arg Thr Pro Ala Ser Thr Pro Cys Arg Pro Asp Ser Ser Arg Ser Ala 100 105 110 Thr Arg Ala Ser His Trp Trp Cys Ser Ser Pro 115 120 3 12 PRT Artificial Synthetic Construct 3 Asn Thr Ser Arg Thr Leu Thr Ala Gly Ala Ala Thr 1 5 10 4 45 PRT Artificial Synthetic Construct 4 Ser Cys Phe Arg Pro Ala Trp Thr Arg Arg Thr Cys Thr Gly Thr Leu 1 5 10 15 Ser Thr Thr Ser Cys Leu Val Leu Thr Ser Val Ala Pro Ala Pro Arg 20 25 30 Arg Phe Thr Ser Ser Ser Thr Thr Arg Ala Arg Thr Cys 35 40 45 5 17 PRT Artificial Synthetic Construct 5 Ser Thr Arg Thr Ser Val Ala Arg Thr Thr Ser Ser His Thr Cys Thr 1 5 10 15 Arg 6 9 PRT Artificial Synthetic Construct 6 Ser Cys Gly Arg Thr Thr Arg Met Arg 1 5 7 23 PRT Artificial Synthetic Construct 7 Arg Leu Thr Thr Ala Arg Trp Ser Arg Ala Pro Trp Arg Met Thr Gly 1 5 10 15 Thr Ser Tyr Pro Pro Arg Arg 20 8 56 PRT Artificial Synthetic Construct 8 Arg Thr Gln Met Pro Arg Ser Leu Lys Thr Gly Thr Ser Gly Pro Arg 1 5 10 15 Ser Thr Thr Pro Arg Thr Pro Ser Pro Arg Thr Gly Thr Ser Pro Ser 20 25 30 Thr Ser Pro Thr Arg Thr Arg Arg Ser Pro Lys Thr Gly Thr Lys Lys 35 40 45 Trp Thr Glu Ser Gly Ser Arg Arg 50 55 9 91 PRT Artificial Synthetic Construct 9 Phe Arg Thr Pro Ser Thr Arg Val Ser Gly Ser Arg Gly Arg Ser Thr 1 5 10 15 Thr Pro Ile Thr Lys Ala Pro Gly Ser Thr Pro Lys Ser Thr Thr Pro 20 25 30 Ser Thr Arg Pro Thr Leu Thr Ser Met Pro Thr Thr Ala Leu Pro Cys 35 40 45 Trp Ala Trp Thr Ser Gly Arg Ser Ser Arg Ala Pro Ser Ser Thr Thr 50 55 60 Ser Ser Ser Pro Thr Met Arg Arg Thr Gln Arg Ser Leu Ala Thr Arg 65 70 75 80 Arg Gly Ala Ser Pro Arg Arg Pro Arg Ser Arg 85 90 10 9 PRT Artificial Synthetic Construct 10 Lys Thr Ser Arg Thr Arg Ser Ser Gly 1 5 11 51 PRT Artificial Synthetic Construct 11 Arg Arg Arg Arg Arg Arg Arg Ser Gly Arg Arg Arg Arg Arg Pro Arg 1 5 10 15 Arg Thr Arg Arg Thr Arg Thr Thr Arg Arg Thr Arg Met Arg Thr Arg 20 25 30 Arg Thr Arg Thr Arg Arg Arg Arg Arg Arg Pro Pro Ala Arg Pro Arg 35 40 45 Thr Ser Cys 50 12 2691 DNA Artificial construct of SM22a promoter and CRT cDNA with HA tag inserted into CRT cDNA 12 ccccttcctt cagatgccac aaggaggtgc tggagttcta tgcaccaata gcttaaacca 60 gccaggctgg ctgtagtgga ttgagcgtct gaggctgcac ctctctggcc tgcagccagt 120 tcctgggtga gactgaccct gcctgagggt tctctccttc cctctctcta ctcctttcct 180 ccctctccct ctccctctct ctgtttcctg aggtttccag gattggggat gggactcaga 240 gacaccacta aagccttacc ttttaagaag ttgcattcag tgagtgtgtg agacatagca 300 cagatagggg cagaggagag ctggttctgt ctccactgtg tttggtcttg ggtactgaac 360 tcagaccatc aggtgtgata gcagttgtct ttaaccctaa ccctgagcct gtctcacctg 420 tcccttccca agaccactga agctaggtgc aagataagtg gggacccttt ctgaggtggt 480 aggatctttc acgataagga ctattttgaa gggagggagg gtgacactgt cctagtcctc 540 ttaccctagt gtcctccagc cttgccaggc cttaaacatc cgcccattgt caccgctcta 600 gaaggggcca gggttgactt gctgctaaac aaggcactcc ctagagaagc acccgctaga 660 agcataccat acctgtgggc aggatgaccc atgttctgcc acgcacttgg tagccttgga 720 aaggccactt tgaacctcaa ttttctcaac tgttaaatgg ggtggtaact gctatctcat 780 aataaagggg aacgtgaaag gaaggcgttt gcatagtgcc tggttgtgca gccaggctgc 840 agtcaagact agttcccacc aactcgattt taaagccttg caagaaggtg gcttgtttgt 900 cccttgcagg ttcctttgtc gggccaaact ctagaatgcc tccccctttc tttctcattg 960 aagagcagac ccaagtccgg gtaacaagga agggtttcag ggtcctgccc ataaaaggtt 1020 tttcccggcc gccctcagca ccgccccgcc ccgacccccg cagcatctcc aaagcatgca 1080 gagaatgtct ccggctgccc ccgacagact gctccaactt ggtgtctttc cccaaatatg 1140 gagcctgtgt ggagtgagtg gggcggcccg gggtggtgag ccaagcagac ttccatgggc 1200 agggaggggc gccagcggac ggcagagggg tgacatcact gcctaggcgg cctttaaacc 1260 cctcacccag ccggcgcccc accgagctcg gatccactag tccagtgtgg tggaattc 1318 atg ctg ctc cct gtg ccg ctg ctg ctc ggc ctg ctc ggc ctg gcc gcc 1366 Met Leu Leu Pro Val Pro Leu Leu Leu Gly Leu Leu Gly Leu Ala Ala 1 5 10 15 gcc gag ccc gtc gtc tac ttc aag gag cag ttt ctg gac gga gat ggg 1414 Ala Glu Pro Val Val Tyr Phe Lys Glu Gln Phe Leu Asp Gly Asp Gly 20 25 30 tgg acc gag cgc tgg atc gaa tcc aaa cac aag tcc gat ttt ggc aaa 1462 Trp Thr Glu Arg Trp Ile Glu Ser Lys His Lys Ser Asp Phe Gly Lys 35 40 45 ttc gtc ctc agt tcg ggc aag ttc tac ggc gat cag gag aaa gat aaa 1510 Phe Val Leu Ser Ser Gly Lys Phe Tyr Gly Asp Gln Glu Lys Asp Lys 50 55 60 ggg ctg cag acc agc cag gac gcc cgc ttc tac gcc ctg tcg gcc cga 1558 Gly Leu Gln Thr Ser Gln Asp Ala Arg Phe Tyr Ala Leu Ser Ala Arg 65 70 75 80 ttc gag ccg ttc agc aac aag ggc cag cca ctg gtg gtg cag cca gcc 1606 Phe Glu Pro Phe Ser Asn Lys Gly Gln Pro Leu Val Val Gln Pro Ala 85 90 95 agg acg ccc gct tct acg ccc tgt cgg ccc gat tcg agc cgt tca gca 1654 Arg Thr Pro Ala Ser Thr Pro Cys Arg Pro Asp Ser Ser Arg Ser Ala 100 105 110 aca agg gcc agc cac tgg tgg tgc agt tca ccg tga aac acg agc aga 1702 Thr Arg Ala Ser His Trp Trp Cys Ser Ser Pro Asn Thr Ser Arg 115 120 125 aca ttg act gcg ggg gcg gct acg tga agc tgt ttc cgg ccg gcc tgg 1750 Thr Leu Thr Ala Gly Ala Ala Thr Ser Cys Phe Arg Pro Ala Trp 130 135 140 acc aga agg aca tgc acg ggg act ctg agt aca aca tca tgt ttg gtc 1798 Thr Arg Arg Thr Cys Thr Gly Thr Leu Ser Thr Thr Ser Cys Leu Val 145 150 155 ctg aca tct gtg gcc ccg gca cca aga agg ttc acg tca tct tca act 1846 Leu Thr Ser Val Ala Pro Ala Pro Arg Arg Phe Thr Ser Ser Ser Thr 160 165 170 aca agg gca aga acg tgc tga tca aca agg aca tcc gtt gca agg acg 1894 Thr Arg Ala Arg Thr Cys Ser Thr Arg Thr Ser Val Ala Arg Thr 175 180 185 acg agt tca cac acc tgt aca cgc tga tcg tgc ggc cgg aca aca cgt 1942 Thr Ser Ser His Thr Cys Thr Arg Ser Cys Gly Arg Thr Thr Arg 190 195 200 atg agg tga aga ttg aca aca gcc agg tgg agt cgg gct ccc tgg agg 1990 Met Arg Arg Leu Thr Thr Ala Arg Trp Ser Arg Ala Pro Trp Arg 205 210 215 atg act ggg act tcc tac ccc cca aga aga taa agg acc cag atg cct 2038 Met Thr Gly Thr Ser Tyr Pro Pro Arg Arg Arg Thr Gln Met Pro 220 225 230 cga agc ctg aag act ggg acg agc ggg cca aga tcg acg acc cca cgg 2086 Arg Ser Leu Lys Thr Gly Thr Ser Gly Pro Arg Ser Thr Thr Pro Arg 235 240 245 250 act cca agc ccg agg act ggg aca agc ccg agc aca tcc ccg acc cgg 2134 Thr Pro Ser Pro Arg Thr Gly Thr Ser Pro Ser Thr Ser Pro Thr Arg 255 260 265 acg cga aga agc ccg aag act ggg acg aag aaa tgg acg gag agt ggg 2182 Thr Arg Arg Ser Pro Lys Thr Gly Thr Lys Lys Trp Thr Glu Ser Gly 270 275 280 agc cgc cgg tga ttc aga acc ccg agt aca agg gtg agt gga agc cgc 2230 Ser Arg Arg Phe Arg Thr Pro Ser Thr Arg Val Ser Gly Ser Arg 285 290 295 ggc aga tcg aca acc ccg att aca aag gca cct gga tcc acc ccg aaa 2278 Gly Arg Ser Thr Thr Pro Ile Thr Lys Ala Pro Gly Ser Thr Pro Lys 300 305 310 tcg aca acc ccg agt act cgc ccg acg cta aca tct atg cct acg aca 2326 Ser Thr Thr Pro Ser Thr Arg Pro Thr Leu Thr Ser Met Pro Thr Thr 315 320 325 gct ttg ccg tgc tgg gct tgg acc tct ggc agg tca agt cgg gca cca 2374 Ala Leu Pro Cys Trp Ala Trp Thr Ser Gly Arg Ser Ser Arg Ala Pro 330 335 340 345 tct tcg aca act tcc tca tca cca acg atg agg cgt acg cag agg agt 2422 Ser Ser Thr Thr Ser Ser Ser Pro Thr Met Arg Arg Thr Gln Arg Ser 350 355 360 ttg gca acg aga cgt ggg gcg tca cca aga cgg ccg aga agc aga tga 2470 Leu Ala Thr Arg Arg Gly Ala Ser Pro Arg Arg Pro Arg Ser Arg 365 370 375 aag aca agc agg acg agg agc agc gga tga agg agg agg agg agg aga 2518 Lys Thr Ser Arg Thr Arg Ser Ser Gly Arg Arg Arg Arg Arg Arg 380 385 390 aga agc gga agg agg agg agg agg ccg agg agg acg agg agg aca agg 2566 Arg Ser Gly Arg Arg Arg Arg Arg Pro Arg Arg Thr Arg Arg Thr Arg 395 400 405 acg aca agg agg acg agg atg agg acg agg agg aca agg acg agg agg 2614 Thr Thr Arg Arg Thr Arg Met Arg Thr Arg Arg Thr Arg Thr Arg Arg 410 415 420 agg agg agg cgg ccg ccg gcc tcg agt acc cat atg atg ttc ctg act 2662 Arg Arg Arg Arg Pro Pro Ala Ser Ser Thr His Met Met Phe Leu Thr 425 430 435 atg cta gac agg cca agg acg agc tgt ag 2691 Met Leu Asp Arg Pro Arg Thr Ser Cys 440 445 13 123 PRT Artificial Synthetic Construct 13 Met Leu Leu Pro Val Pro Leu Leu Leu Gly Leu Leu Gly Leu Ala Ala 1 5 10 15 Ala Glu Pro Val Val Tyr Phe Lys Glu Gln Phe Leu Asp Gly Asp Gly 20 25 30 Trp Thr Glu Arg Trp Ile Glu Ser Lys His Lys Ser Asp Phe Gly Lys 35 40 45 Phe Val Leu Ser Ser Gly Lys Phe Tyr Gly Asp Gln Glu Lys Asp Lys 50 55 60 Gly Leu Gln Thr Ser Gln Asp Ala Arg Phe Tyr Ala Leu Ser Ala Arg 65 70 75 80 Phe Glu Pro Phe Ser Asn Lys Gly Gln Pro Leu Val Val Gln Pro Ala 85 90 95 Arg Thr Pro Ala Ser Thr Pro Cys Arg Pro Asp Ser Ser Arg Ser Ala 100 105 110 Thr Arg Ala Ser His Trp Trp Cys Ser Ser Pro 115 120 14 12 PRT Artificial Synthetic Construct 14 Asn Thr Ser Arg Thr Leu Thr Ala Gly Ala Ala Thr 1 5 10 15 45 PRT Artificial Synthetic Construct 15 Ser Cys Phe Arg Pro Ala Trp Thr Arg Arg Thr Cys Thr Gly Thr Leu 1 5 10 15 Ser Thr Thr Ser Cys Leu Val Leu Thr Ser Val Ala Pro Ala Pro Arg 20 25 30 Arg Phe Thr Ser Ser Ser Thr Thr Arg Ala Arg Thr Cys 35 40 45 16 17 PRT Artificial Synthetic Construct 16 Ser Thr Arg Thr Ser Val Ala Arg Thr Thr Ser Ser His Thr Cys Thr 1 5 10 15 Arg 17 9 PRT Artificial Synthetic Construct 17 Ser Cys Gly Arg Thr Thr Arg Met Arg 1 5 18 23 PRT Artificial Synthetic Construct 18 Arg Leu Thr Thr Ala Arg Trp Ser Arg Ala Pro Trp Arg Met Thr Gly 1 5 10 15 Thr Ser Tyr Pro Pro Arg Arg 20 19 56 PRT Artificial Synthetic Construct 19 Arg Thr Gln Met Pro Arg Ser Leu Lys Thr Gly Thr Ser Gly Pro Arg 1 5 10 15 Ser Thr Thr Pro Arg Thr Pro Ser Pro Arg Thr Gly Thr Ser Pro Ser 20 25 30 Thr Ser Pro Thr Arg Thr Arg Arg Ser Pro Lys Thr Gly Thr Lys Lys 35 40 45 Trp Thr Glu Ser Gly Ser Arg Arg 50 55 20 91 PRT Artificial Synthetic Construct 20 Phe Arg Thr Pro Ser Thr Arg Val Ser Gly Ser Arg Gly Arg Ser Thr 1 5 10 15 Thr Pro Ile Thr Lys Ala Pro Gly Ser Thr Pro Lys Ser Thr Thr Pro 20 25 30 Ser Thr Arg Pro Thr Leu Thr Ser Met Pro Thr Thr Ala Leu Pro Cys 35 40 45 Trp Ala Trp Thr Ser Gly Arg Ser Ser Arg Ala Pro Ser Ser Thr Thr 50 55 60 Ser Ser Ser Pro Thr Met Arg Arg Thr Gln Arg Ser Leu Ala Thr Arg 65 70 75 80 Arg Gly Ala Ser Pro Arg Arg Pro Arg Ser Arg 85 90 21 9 PRT Artificial Synthetic Construct 21 Lys Thr Ser Arg Thr Arg Ser Ser Gly 1 5 22 63 PRT Artificial Synthetic Construct 22 Arg Arg Arg Arg Arg Arg Arg Ser Gly Arg Arg Arg Arg Arg Pro Arg 1 5 10 15 Arg Thr Arg Arg Thr Arg Thr Thr Arg Arg Thr Arg Met Arg Thr Arg 20 25 30 Arg Thr Arg Thr Arg Arg Arg Arg Arg Arg Pro Pro Ala Ser Ser Thr 35 40 45 His Met Met Phe Leu Thr Met Leu Asp Arg Pro Arg Thr Ser Cys 50 55 60 23 418 PRT Artificial CRT peptide sequence from CRT cDNA 23 Met Leu Leu Pro Val Pro Leu Leu Leu Gly Leu Leu Gly Leu Ala Ala 1 5 10 15 Ala Glu Pro Val Val Tyr Phe Lys Glu Gln Phe Leu Asp Gly Asp Gly 20 25 30 Trp Thr Glu Arg Trp Ile Glu Ser Lys His Lys Ser Asp Phe Gly Lys 35 40 45 Phe Val Leu Ser Ser Gly Lys Phe Tyr Gly Asp Gln Glu Lys Asp Lys 50 55 60 Gly Leu Gln Thr Ser Gln Asp Ala Arg Phe Tyr Ala Leu Ser Ala Arg 65 70 75 80 Phe Glu Pro Phe Ser Asn Lys Gly Gln Pro Leu Val Val Gln Phe Thr 85 90 95 Val Lys His Glu Gln Asn Ile Asp Cys Gly Gly Gly Tyr Val Lys Leu 100 105 110 Phe Pro Ala Gly Leu Asp Gln Lys Asp Met His Gly Asp Ser Glu Tyr 115 120 125 Asn Ile Met Phe Gly Pro Asp Ile Cys Gly Pro Gly Thr Lys Lys Val 130 135 140 His Val Ile Phe Asn Tyr Lys Gly Lys Asn Val Leu Ile Asn Lys Asp 145 150 155 160 Ile Arg Cys Lys Asp Asp Glu Phe Thr His Leu Tyr Thr Leu Ile Val 165 170 175 Arg Pro Asp Asn Thr Tyr Glu Val Lys Ile Asp Asn Ser Gln Val Glu 180 185 190 Ser Gly Ser Leu Glu Asp Asp Trp Asp Phe Leu Pro Pro Lys Lys Ile 195 200 205 Lys Asp Pro Asp Ala Ser Lys Pro Glu Asp Trp Asp Glu Arg Ala Lys 210 215 220 Ile Asp Asp Pro Thr Asp Ser Lys Pro Glu Asp Trp Asp Lys Pro Glu 225 230 235 240 His Ile Pro Asp Pro Asp Ala Lys Lys Pro Glu Asp Trp Asp Glu Glu 245 250 255 Met Asp Gly Glu Trp Glu Pro Pro Val Ile Gln Asn Pro Glu Tyr Lys 260 265 270 Gly Glu Trp Lys Pro Arg Gln Ile Asp Asn Pro Asp Tyr Lys Gly Thr 275 280 285 Trp Ile His Pro Glu Ile Asp Asn Pro Glu Tyr Ser Pro Asp Ala Asn 290 295 300 Ile Tyr Ala Tyr Asp Ser Phe Ala Val Leu Gly Leu Asp Leu Trp Gln 305 310 315 320 Val Lys Ser Gly Thr Ile Phe Asp Asn Phe Leu Ile Thr Asn Asp Glu 325 330 335 Ala Tyr Ala Glu Glu Phe Gly Asn Glu Thr Trp Gly Val Thr Lys Thr 340 345 350 Ala Glu Lys Gln Met Lys Asp Lys Gln Asp Glu Glu Gln Arg Leu Lys 355 360 365 Glu Glu Glu Glu Glu Lys Lys Arg Lys Glu Glu Glu Glu Ala Glu Glu 370 375 380 Asp Glu Glu Asp Lys Asp Asp Lys Glu Asp Glu Asp Glu Asp Glu Glu 385 390 395 400 Asp Lys Asp Glu Glu Glu Glu Glu Ala Ala Ala Gly Gln Ala Lys Asp 405 410 415 Glu Leu 24 430 PRT Artificial CRT peptide sequence with HA tag inserted into peptide 24 Met Leu Leu Pro Val Pro Leu Leu Leu Gly Leu Leu Gly Leu Ala Ala 1 5 10 15 Ala Glu Pro Val Val Tyr Phe Lys Glu Gln Phe Leu Asp Gly Asp Gly 20 25 30 Trp Thr Glu Arg Trp Ile Glu Ser Lys His Lys Ser Asp Phe Gly Lys 35 40 45 Phe Val Leu Ser Ser Gly Lys Phe Tyr Gly Asp Gln Glu Lys Asp Lys 50 55 60 Gly Leu Gln Thr Ser Gln Asp Ala Arg Phe Tyr Ala Leu Ser Ala Arg 65 70 75 80 Phe Glu Pro Phe Ser Asn Lys Gly Gln Pro Leu Val Val Gln Phe Thr 85 90 95 Val Lys His Glu Gln Asn Ile Asp Cys Gly Gly Gly Tyr Val Lys Leu 100 105 110 Phe Pro Ala Gly Leu Asp Gln Lys Asp Met His Gly Asp Ser Glu Tyr 115 120 125 Asn Ile Met Phe Gly Pro Asp Ile Cys Gly Pro Gly Thr Lys Lys Val 130 135 140 His Val Ile Phe Asn Tyr Lys Gly Lys Asn Val Leu Ile Asn Lys Asp 145 150 155 160 Ile Arg Cys Lys Asp Asp Glu Phe Thr His Leu Tyr Thr Leu Ile Val 165 170 175 Arg Pro Asp Asn Thr Tyr Glu Val Lys Ile Asp Asn Ser Gln Val Glu 180 185 190 Ser Gly Ser Leu Glu Asp Asp Trp Asp Phe Leu Pro Pro Lys Lys Ile 195 200 205 Lys Asp Pro Asp Ala Ser Lys Pro Glu Asp Trp Asp Glu Arg Ala Lys 210 215 220 Ile Asp Asp Pro Thr Asp Ser Lys Pro Glu Asp Trp Asp Lys Pro Glu 225 230 235 240 His Ile Pro Asp Pro Asp Ala Lys Lys Pro Glu Asp Trp Asp Glu Glu 245 250 255 Met Asp Gly Glu Trp Glu Pro Pro Val Ile Gln Asn Pro Glu Tyr Lys 260 265 270 Gly Glu Trp Lys Pro Arg Gln Ile Asp Asn Pro Asp Tyr Lys Gly Thr 275 280 285 Trp Ile His Pro Glu Ile Asp Asn Pro Glu Tyr Ser Pro Asp Ala Asn 290 295 300 Ile Tyr Ala Tyr Asp Ser Phe Ala Val Leu Gly Leu Asp Leu Trp Gln 305 310 315 320 Val Lys Ser Gly Thr Ile Phe Asp Asn Phe Leu Ile Thr Asn Asp Glu 325 330 335 Ala Tyr Ala Glu Glu Phe Gly Asn Glu Thr Trp Gly Val Thr Lys Thr 340 345 350 Ala Glu Lys Gln Met Lys Asp Lys Gln Asp Glu Glu Gln Arg Leu Lys 355 360 365 Glu Glu Glu Glu Glu Lys Lys Arg Lys Glu Glu Glu Glu Ala Glu Glu 370 375 380 Asp Glu Glu Asp Lys Asp Asp Lys Glu Asp Glu Asp Glu Asp Glu Glu 385 390 395 400 Asp Lys Asp Glu Glu Glu Glu Glu Ala Ala Ala Gly Leu Glu Tyr Pro 405 410 415 Tyr Asp Val Pro Asp Tyr Ala Arg Gln Ala Lys Asp Glu Leu 420 425 430 

1. A transgenic mouse whose genome comprises a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin (CRT) wherein said control region comprises a promoter wherein expression of calreticulin in the vascular smooth muscle cells results in hemangioma formation.
 2. The transgenic mouse according to claim 1 wherein the promoter is SM22α promoter.
 3. A transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin wherein said control region comprises a SM22α promoter.
 4. A method for producing a transgenic mouse whose genome comprises CRT comprising: introducing into a fertilized mouse egg a transgene comprising a transcriptional control region operably linked to a cDNA encoding CRT wherein said control region comprises a promoter; transplanting the injected egg in a foster parent female mouse; and selecting a mouse derived from an injected egg whose genome comprises CRT.
 5. The method according to claim 4 wherein the promoter comprises SM22α promoter.
 6. A method for screening compounds that inhibit vascular tumor formation in a transgenic mouse comprising providing a transgenic mouse whose genome comprises a transgene comprising a transcriptional control region operably linked to a cDNA encoding calreticulin (CRT); allowing CRT to be expressed in said transgenic mouse administering a compound to said mouse; and determining whether said compound reduces hemangioma formation.
 7. A compound isolated according to the method of claim
 6. 8. A method of testing the therapeutic activity of a pharmacological agent on Kaposiform hemangioenothelioma comprising administering an effective amount of said pharmacological agent to the mouse of claim 1 and evaluating said agent's effect on hemangioma formation of said mouse.
 9. A compound isolated according to the method of claim
 8. 10. A method of inhibiting hemangioma formation comprising administering an effective amount of a matrix metalloproteinase inhibitor to a patient in need of such treatment.
 11. A method of inhibiting hemangioma comprising administering to an individual in need of such treatment an effective amount of virally-administered small interference RNA (siRNA) corresponding to a portion of CRT mRNA, wherein expression of the siRNA decreases the level of CRT. 